Catalog Number

-

Brand Name

Non-Rotatable Snares

Version/Model Number

MD-E-SNC243224

Device Commercial Distribution Status

In Commercial Distribution

Commercial Distribution End Date

-

Issuing Agency

In GS1

MRI safety Status

Labeling does not contain MRI Safety Information

Device required to be labeled as containing natural rubber latex or dry natural rubber (21 CFR 801.437)

-

Device labeled as "Not made with natural rubber latex"

-

For Single-Use

Yes

Prescription Use (Rx)

Yes

Over the Counter (OTC)

-

Kit

-

Combination Product

-

Human Cell, Tissue or Cellular or Tissue-Based Product (HCT/P)

-

FDA Premarket Submission

K172758,K172758,K172758

Product Code

FDI

Product Code Name

Snare, Flexible

Public Device Record Key

ff1bbe39-e1b1-489c-932a-edcb3abfbad2

Public Version Date

July 18, 2022

Public Version Number

3

DI Record Publish Date

October 23, 2019

Package DI Number

26970401814262

Quantity per Package

5

Contains DI Package

16970401814258

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

Caxe